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  4. NDC Product Code: 65734-511 Isodine Copitos

NDC 65734-511 Isodine Copitos

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 65734-511?
  5. Isodine Copitos Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
65734-511
Proprietary Name:
Isodine Copitos
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Swabplus Inc.
Labeler Code:
65734
Product Label ID:
8629d5dd-2a59-4184-89e5-d63b77e66226
Start Marketing Date: [9]
06-01-2008
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - DARK)

Code Structure Chart

Product Details

What is NDC 65734-511?

The NDC code 65734-511 is assigned by the FDA to the product Isodine Copitos which is product labeled by Swabplus Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 65734-511-72 72 applicator in 1 package / .15 ml in 1 applicator (65734-511-00). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Isodine Copitos?

Hold the swab vertically, with the color ring tip upwards, Hold n the center of the tube with one hand at the color ring with the other.Gently snap the tip with the color ring, Formula inside the tube flows down and fills the opposite tip.Apply the product to the affected area.Discard swab after use.

Which are Isodine Copitos UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Isodine Copitos Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Isodine Copitos?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".